rs730881710

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(TC;TC)	0	common in clinvar

Make rs730881710(-;-)

Make rs730881710(-;TC)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

95107211

Gene	C9orf3, FANCC, LOC107987102

is a	snp
is	mentioned by
dbSNP	rs730881710
dbSNP (classic)	rs730881710
ClinGen	rs730881710
ebi	rs730881710
HLI	rs730881710
Exac	rs730881710
Gnomad	rs730881710
Varsome	rs730881710
LitVar	rs730881710
Map	rs730881710
PheGenI	rs730881710
Biobank	rs730881710
1000 genomes	rs730881710
hgdp	rs730881710
ensembl	rs730881710
geneview	rs730881710
scholar	rs730881710
google	rs730881710
pharmgkb	rs730881710
gwascentral	rs730881710
openSNP	rs730881710
23andMe	rs730881710
SNPshot	rs730881710
SNPdbe	rs730881710
MSV3d	rs730881710
GWAS Ctlg	rs730881710

Max Magnitude

0

ClinVar
Risk	rs730881710(-;-)
Alt	rs730881710(-;-)
Reference	Rs730881710(TC;TC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	FANCC
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000009.11:g.97869493_97869494delGA
CLNSRC
CLNACC	RCV000160469.1,